排序方式: 共有48条查询结果,搜索用时 15 毫秒
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采用少量高分子量聚乙烯(HMWPE)在动态保压剪切应力场中诱导中等分子量聚乙烯(MMWPE),在这种双重诱导的作用下得到了性能良好的聚乙烯材料,其平行于流动方向的拉伸强度和冲击强度达到了71.17 MPa和75.79 kJ/m<'2>,分别提高了209.4%和252.8%;通过差示扫描量热(DSC),X射线衍射(WAX... 相似文献
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在成型过程中向成型设备或模具分别输入具有不同振频和振幅的振动场、不同拉伸比的拉伸应力场、不同剪切速率的剪应力场、以及先剪切后拉伸的复合应力场等,成功地改变了聚合物凝聚态结构;改变了结晶聚合物的结晶度、取向度、晶粒尺寸、晶胞参数;生成了不同的串晶结构、串晶互锁结构。分别得到了具有突出高强度、高模量的试样,自增强同时又自增韧的试样,在单方向应力场中获得双向自增强结构的试样,以及在极少量高分子组分诱导下性能大幅度提高的试样。 相似文献
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利用低频熔体振动注射成型技术获得自增强高密度聚乙烯。实验结果表明,采用振动注射成型工艺,试样屈服拉伸强度由26.5MPa提高到36.1MPa;试样的芯层中可获取沿流动方向生成的串晶或行式排列的片晶结构;压力振动注射有利于分子在(110)晶面择优取向,使结晶更加完善;振动注射提高了试样的结晶度,芯层结晶度最大提高了10.2%。 相似文献
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聚乙烯增强增韧改性进展 总被引:5,自引:0,他引:5
论述刚性无机粒子、纳米材料、晶须、离聚体和聚酯短纤维对聚乙烯的增强增韧改性,以及聚乙烯的自增强增韧行为,并介绍改性聚乙烯的性能和改性机理。 相似文献
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Wei Meifen; Mallinckrodt Brent; Larson Lisa M.; Zakalik Robyn A. 《Canadian Metallurgical Quarterly》2005,52(3):368
Attachment working models of self and others may govern adults' preferences for internal vs. external sources of reassurance, which, if unavailable, lead to depressive symptoms. This study examined a model in which the link between depressive symptoms and attachment anxiety is mediated by (a) capacity for self-reinforcement and (b) need for reassurance from others, whereas the link between depressive symptoms and attachment avoidance is mediated only by the capacity for self-reinforcement. Analysis of survey data from 425 undergraduates indicated that both capacity for self-reinforcement and need for reassurance from others partially mediated the link between attachment anxiety and depression. Capacity for self-reinforcement fully mediated the link between attachment avoidance and depression. Moreover, 54% of the variance in depressive symptoms was explained by attachment anxiety, self-reinforcement, and need for reassurance from others. (PsycINFO Database Record (c) 2010 APA, all rights reserved) 相似文献
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Weijun Yang Yanlin Zhu Tianxi Liu Debora Puglia Jose M. Kenny Pengwu Xu Rui Zhang Piming Ma 《Advanced functional materials》2023,33(12):2213294
High-performance elastomers are expected to possess excellent healing and recycling ability, damage resistance in conjunction with high strength and toughness. Herein, a dual dynamic crosslinking strategy is implemented by multiple hydrogen and disulfide bonds to obtain a novel amorphous and transparent polyurethane/nanocellulose elastomer with excellent self-healing, self-reinforcing and toughening performance. First, hydrogen bonds are introduced in TEMPO-oxidized cellulose nanofibers (TCNF) by modification with 2-ureido-4[1H]-pyrimidone (UTCNF), while disulfide bonds (SS) are introduced in the polyurethane (PU) main chain, leading to the formation of dual dynamic cross-linking networks. The PU-SS-UTCNF elastomer can fully self-heal within 4.0 h at 50 °C. Surprisingly, for the first time, the PU-SS-UTCNF elastomer also self-strengthens and self-toughens after multiple hot-pressing, with tensile strength and toughness that increase by up to 401% and 257% compared to original elastomer samples, up to 50.0 MPa and 132.5 MJ m-3. The self-strength and self-toughening effects are attributed to 1) reconstruction of dual dynamic networks that increase the cross-linking degree during the multiple hot-pressing processes; 2) multiple hydrogen bonds in the system are beneficial to the orientation of highly crystallized UTCNF, as a replacement of stress-induced process in deformation under external tensile force. 相似文献
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自增强HDPE棒材的结构及力学性能 总被引:2,自引:0,他引:2
通过扫描电子显微镜、差示扫描量热法、广角X射线衍射分析与力学性能测试,研究了自增强高密度聚乙烯(HDPE)棒材微观结构特点和力学性能。结果表明,自增强HDPE棒材呈现明显的皮芯结构,表皮的结晶度高达75.88%,芯部的组织和结构与普通注塑试样最相近;与普通HDPE试样相比,自增强HDPE棒材的微晶尺寸和结晶度大幅提高,晶面间距几乎未变化,内部存在大量的微纤结构。制备的自增强HDPE棒材的拉伸强度和弯曲强度分别为220.6 MPa和152.9 MPa,均为未增强试样的近10倍。 相似文献
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This article provides a method to obtain high-hoop-strength high-density polyethylene (HDPE) pipe by mandrel-rotating extrusion. With properly selected processing temperature, pressure, and mandrel-rotating speed, the hoop strength of 90 Mpa has been got. Differential scanning calorimetry and X-ray scattering found the great strength enhancement was owning to high degree of macromolecular orientation in circumferential direction and the shish-kebab structure. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 323–328, 1998 相似文献
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